| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2857595 | 0.827 | 0.320 | 6 | 31600692 | intergenic variant | G/A | snv | 0.27 | 6 | ||
| rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 5 | ||
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 4 | |
| rs2284746 | 1 | 16980180 | intron variant | C/A;G | snv | 4 | |||||
| rs1036429 | 12 | 95877650 | intron variant | T/C | snv | 0.79 | 3 | ||||
| rs11001819 | 10 | 76555466 | intron variant | G/A | snv | 0.41 | 3 | ||||
| rs11168048 | 5 | 148462790 | intron variant | T/C | snv | 0.38 | 3 | ||||
| rs12447804 | 16 | 58041378 | intron variant | C/T | snv | 0.18 | 3 | ||||
| rs12477314 | 2 | 238955452 | regulatory region variant | C/G;T | snv | 3 | |||||
| rs12899618 | 15 | 71352781 | intron variant | G/A | snv | 0.14 | 3 | ||||
| rs1435867 | 2 | 228646213 | intron variant | T/C | snv | 7.3E-02 | 3 | ||||
| rs1529672 | 1.000 | 0.040 | 3 | 25479091 | intron variant | C/A;T | snv | 3 | |||
| rs16909898 | 9 | 95468726 | intron variant | A/G | snv | 8.4E-02 | 0.10 | 3 | |||
| rs17331332 | 4 | 105886950 | intron variant | G/A | snv | 4.5E-02 | 3 | ||||
| rs1928168 | 6 | 22017509 | intron variant | T/C | snv | 0.36 | 3 | ||||
| rs1980057 | 1.000 | 0.040 | 4 | 144564586 | intron variant | C/T | snv | 0.31 | 3 | ||
| rs2277027 | 5 | 157505368 | intron variant | A/C | snv | 0.42 | 3 | ||||
| rs2571445 | 0.925 | 0.080 | 2 | 217818431 | missense variant | A/G;T | snv | 0.62 | 3 | ||
| rs2798641 | 6 | 108946847 | intron variant | C/T | snv | 0.15 | 3 | ||||
| rs2865531 | 1.000 | 0.040 | 16 | 75356418 | intron variant | T/A | snv | 0.52 | 3 | ||
| rs3817928 | 6 | 142429379 | intron variant | A/G | snv | 0.20 | 3 | ||||
| rs7068966 | 1.000 | 0.040 | 10 | 12235993 | intron variant | C/T | snv | 0.43 | 3 |